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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Catheter, Assisted Reproduction
510(k) Number K990348
Device Name WALLACE TRIAL TRANSFER CATHETER, MODEL TT 1816N
Applicant
CooperSurgical, Inc.
15 Forest Pkwy.
Shelton,  CT  06484
Applicant Contact DEBRA A PEKAR
Correspondent
CooperSurgical, Inc.
15 Forest Pkwy.
Shelton,  CT  06484
Correspondent Contact DEBRA A PEKAR
Regulation Number884.6110
Classification Product Code
MQF  
Date Received02/05/1999
Decision Date 07/26/1999
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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